164 related articles for article (PubMed ID: 765939)
1. [Alport's-syndrome: diagnosis, light- and electronmicroscopic findings (author's transl)].
Balzar E; Lubec G; Syŕe G; Weissenbacher G
Padiatr Padol; 1976; 11(1):221-33. PubMed ID: 765939
[TBL] [Abstract][Full Text] [Related]
2. [Diagnostic progress in familial nephropathy. Alport's syndrome, nail-patella syndrome and benign familial hematuria (author's transl)].
Spichtin H; Mihatsch MJ
Pathol Res Pract; 1979 Apr; 164(1):80-6. PubMed ID: 461223
[TBL] [Abstract][Full Text] [Related]
3. Alport's syndrome (progressive hereditary nephritis).
Gaboardi F; Edefonti A; Imbasciati E; Tarantino A; Mihatsch MJ; Zollinger HU
Clin Nephrol; 1974; 2(4):143-56. PubMed ID: 4603152
[No Abstract] [Full Text] [Related]
4. Recent developments in hereditary nephritis (Alport's syndrome).
Bubalo FS; Davidson DD
Indiana Med; 1991 Dec; 84(12):860-6. PubMed ID: 1774457
[TBL] [Abstract][Full Text] [Related]
5. [Significance of family studies and kidney biopsies in children with renal hematuria].
Pistor K; Bachmann H; Rumpelt HJ; Olbing H
Monatsschr Kinderheilkd; 1985 May; 133(5):269-73. PubMed ID: 4010678
[TBL] [Abstract][Full Text] [Related]
6. Alport's syndrome. Emphasizing electron microscopic studies of the glomerulus.
Spear GS; Slusser RJ
Am J Pathol; 1972 Nov; 69(2):213-24. PubMed ID: 4343992
[TBL] [Abstract][Full Text] [Related]
7. Basement membrane nephropathy: a new classification for Alport's syndrome and asymptomatic hematuria based on ultrastructural findings.
Yum M; Bergstein JM
Hum Pathol; 1983 Nov; 14(11):996-1003. PubMed ID: 6629370
[TBL] [Abstract][Full Text] [Related]
8. Thin glomerular basement membrane disease: clinical significance of a morphological diagnosis--a collaborative study of the Italian Renal Immunopathology Group.
Frascà GM; Onetti-Muda A; Mari F; Longo I; Scala E; Pescucci C; Roccatello D; Alpa M; Coppo R; Li Volti G; Feriozzi S; Bergesio F; Schena FP; Renieri A;
Nephrol Dial Transplant; 2005 Mar; 20(3):545-51. PubMed ID: 15618242
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant Alport's syndrome: study of a large Tunisian family.
Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J
Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251
[TBL] [Abstract][Full Text] [Related]
10. Characteristic ultrastructural lesion of the glomerular basement membrane in progressive hereditary nephritis (Alport's syndrome).
Hinglais N; Grünfeld JP; Bois E
Lab Invest; 1972 Nov; 27(5):473-87. PubMed ID: 4653971
[No Abstract] [Full Text] [Related]
11. [Epidemiological study in 4 family units with Alport's syndrome].
García-Delgado C; Gordillo-Paniagua G
Bol Med Hosp Infant Mex; 1981; 38(6):887-902. PubMed ID: 7317143
[TBL] [Abstract][Full Text] [Related]
12. [Morphological changes in the inner ear of alport's syndrome (author's transl)].
Weidauer H; Arnold W
Laryngol Rhinol Otol (Stuttg); 1976 Jan; 55(1):6-16. PubMed ID: 134197
[TBL] [Abstract][Full Text] [Related]
13. [3 cases of Alport's syndrome with different clinical and morphologic manifestations].
Bechcińska B; Danilewicz M; Kałuzyński A; Marek K; Wagrowska-Danilewicz M
Patol Pol; 1989; 40(1):123-8. PubMed ID: 2477788
[TBL] [Abstract][Full Text] [Related]
14. [The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion].
Tsalikova FD; Ignatova MS; Krasnopol'skaia KD; Tverskaia SM; Brydun AV
Ter Arkh; 1995; 67(4):45-7. PubMed ID: 7784975
[TBL] [Abstract][Full Text] [Related]
15. A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome.
Dagher H; Buzza M; Colville D; Jones C; Powell H; Fassett R; Wilson D; Agar J; Savige J
Am J Kidney Dis; 2001 Dec; 38(6):1217-28. PubMed ID: 11728953
[TBL] [Abstract][Full Text] [Related]
16. [Recurrent hematuria in children].
Dumas R; Baldet P; Bascoul S; Serres L; Jean R
Arch Fr Pediatr; 1978; 35(7):737-55. PubMed ID: 736729
[TBL] [Abstract][Full Text] [Related]
17. Familial thin basement membrane nephropathy in children with asymptomatic microhematuria.
Gauthier B; Trachtman H; Frank R; Valderrama E
Nephron; 1989; 51(4):502-8. PubMed ID: 2739828
[TBL] [Abstract][Full Text] [Related]
18. [Alport's Syndrome. Hereditary nephritis, perceptive deafness and lens anomalies].
Norrelund N
Ugeskr Laeger; 1971 Mar; 133(11):503-5. PubMed ID: 5092560
[No Abstract] [Full Text] [Related]
19. A Sri Lankan family with Alport's syndrome.
Angunawela P; Mahamiththawa U
Ceylon Med J; 1998 Mar; 43(1):56-7. PubMed ID: 9624855
[No Abstract] [Full Text] [Related]
20. Alport's syndrome: experience at Hôpital Necker.
Habib R; Gubler MC; Hinglais N; Noël LH; Droz D; Levy M; Mahieu P; Foidart JM; Perrin D; Bois E; Grünfeld JP
Kidney Int Suppl; 1982 May; 11():S20-8. PubMed ID: 6956772
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]